Variant report

Variant	esv1803077
Chromosome Location	chr10:21878144-22013644
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1231)
CpG islands
(count:183)
Chromatin interactive
region (count:109)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1231 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:22013360-22013970	K562	blood:	n/a	n/a
2	ARID3A	chr10:22013511-22014320	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:21912298-21912489	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:21950782-21950786	K562	blood:	n/a	n/a
5	ARID3A	chr10:21955681-21955702	K562	blood:	n/a	n/a
6	ARID3A	chr10:21964142-21964505	HepG2	liver:	n/a	n/a
7	ATF1	chr10:22009018-22009361	K562	blood:	n/a	n/a
8	ATF1	chr10:21976658-21976858	K562	blood:	n/a	n/a
9	ATF1	chr10:21950124-21950374	K562	blood:	n/a	n/a
10	ATF1	chr10:22013180-22013997	K562	blood:	n/a	n/a
11	ATF1	chr10:21944988-21945293	K562	blood:	n/a	n/a
12	ATF1	chr10:21991603-21991760	K562	blood:	n/a	n/a
13	ATF2	chr10:21999461-22000047	GM12878	blood:	n/a	n/a
14	ATF2	chr10:21991403-21992133	GM12878	blood:	n/a	n/a
15	ATF2	chr10:21999479-22000064	GM12878	blood:	n/a	n/a
16	ATF2	chr10:21991423-21992167	GM12878	blood:	n/a	n/a
17	ATF3	chr10:22013564-22013930	K562	blood:	n/a	n/a
18	BACH1	chr10:21995995-21995999	K562	blood:	n/a	n/a
19	BACH1	chr10:21975911-21975997	K562	blood:	n/a	n/a
20	BATF	chr10:21999624-21999995	GM12878	blood:	n/a	n/a
21	BATF	chr10:22013608-22013889	GM12878	blood:	n/a	n/a
22	BCL11A	chr10:21999723-22000032	GM12878	blood:	n/a	n/a
23	BCL3	chr10:22013383-22014056	A549	lung:	n/a	n/a
24	BCLAF1	chr10:21991700-21992222	GM12878	blood:	n/a	n/a
25	BHLHE40	chr10:21999562-21999999	GM12878	blood:	n/a	n/a
26	BHLHE40	chr10:22009095-22009442	GM12878	blood:	n/a	n/a
27	BRCA1	chr10:21938750-21938763	GM12878	blood:	n/a	n/a
28	BRCA1	chr10:21937177-21937201	H1-hESC	embryonic stem cell:	n/a	n/a
29	CBX3	chr10:21989357-21989806	K562	blood:	n/a	n/a
30	CBX3	chr10:21989263-21989756	K562	blood:	n/a	n/a
31	CBX3	chr10:21896856-21897194	K562	blood:	n/a	n/a
32	CCNT2	chr10:22013459-22013981	K562	blood:	n/a	n/a
33	CCNT2	chr10:21990699-21990809	K562	blood:	n/a	n/a
34	CEBPB	chr10:21966520-21966829	IMR90	lung:	n/a	chr10:21966655-21966672 chr10:21966658-21966669
35	CEBPB	chr10:21996348-21996664	MCF-7	breast:	n/a	chr10:21996517-21996528
36	CEBPB	chr10:21966511-21966811	HepG2	liver:	n/a	chr10:21966655-21966672 chr10:21966658-21966669
37	CEBPB	chr10:21906213-21906580	IMR90	lung:	n/a	n/a
38	CEBPB	chr10:21906255-21906506	MCF-7	breast:	n/a	n/a
39	CEBPB	chr10:22013569-22013867	HepG2	liver:	n/a	chr10:22013720-22013733 chr10:22013717-22013734 chr10:22013722-22013731 chr10:22013721-22013732 chr10:22013722-22013731 chr10:22013722-22013731
40	CEBPB	chr10:21996431-21996702	IMR90	lung:	n/a	chr10:21996517-21996528
41	CEBPB	chr10:22013169-22014121	K562	blood:	n/a	chr10:22013720-22013733 chr10:22013717-22013734 chr10:22014078-22014091 chr10:22013722-22013731 chr10:22013721-22013732 chr10:22013722-22013731 chr10:22013722-22013731
42	CEBPB	chr10:22013447-22014059	MCF-7	breast:	n/a	chr10:22013720-22013733 chr10:22013717-22013734 chr10:22013722-22013731 chr10:22013721-22013732 chr10:22013722-22013731 chr10:22013722-22013731
43	CEBPB	chr10:21957836-21958130	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr10:22013381-22014050	HCT-116	colon:	n/a	chr10:22013720-22013733 chr10:22013717-22013734 chr10:22013722-22013731 chr10:22013721-22013732 chr10:22013722-22013731 chr10:22013722-22013731
45	CEBPB	chr10:21906216-21906583	HepG2	liver:	n/a	n/a
46	CEBPB	chr10:21935021-21935058	A549	lung:	n/a	n/a
47	CEBPB	chr10:22013548-22013926	K562	blood:	n/a	chr10:22013720-22013733 chr10:22013717-22013734 chr10:22013722-22013731 chr10:22013721-22013732 chr10:22013722-22013731 chr10:22013722-22013731
48	CEBPB	chr10:21976654-21976900	A549	lung:	n/a	n/a
49	CEBPB	chr10:22001673-22001761	K562	blood:	n/a	chr10:22001714-22001725
50	CEBPB	chr10:22013577-22013944	GM12878	blood:	n/a	chr10:22013720-22013733 chr10:22013717-22013734 chr10:22013722-22013731 chr10:22013721-22013732 chr10:22013722-22013731 chr10:22013722-22013731

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:21958473-21958523	HCT-116	colon:	n/a
2	chr10:21926911-21926961	HCPEpiC	choroid plexus:	n/a
3	chr10:21958473-21958523	HEEpiC	esophagus:	n/a
4	chr10:21926911-21926961	Hela-S3	cervix:	n/a
5	chr10:21982589-21982639	AG10803	skin:	n/a
6	chr10:21926911-21926961	HCM	heart:	n/a
7	chr10:21926911-21926961	HUVEC	blood vessel:	n/a
8	chr10:21958473-21958523	GM06990	blood:	n/a
9	chr10:21926911-21926961	ProgFib	skin:	n/a
10	chr10:21926911-21926961	SK-N-SH	brain:	n/a
11	chr10:21982589-21982639	AG04450	lung:	fetal
12	chr10:21926911-21926961	NB4	blood:	n/a
13	chr10:21926911-21926961	SK-N-SH_RA	brain:	n/a
14	chr10:21982589-21982639	HRE	kidney:	n/a
15	chr10:21958473-21958523	SK-N-SH	brain:	n/a
16	chr10:21958473-21958523	IMR90	lung:	fetal
17	chr10:21926911-21926961	HRCEpiC	kidney:	n/a
18	chr10:21926911-21926961	BJ	skin:	n/a
19	chr10:21958473-21958523	HUVEC	blood vessel:	n/a
20	chr10:21982589-21982639	NB4	blood:	n/a
21	chr10:21926911-21926961	PFSK-1	brain:	n/a
22	chr10:21958473-21958523	HPAEpiC	pulmonary alveolar:	n/a
23	chr10:21982589-21982639	GM06990	blood:	n/a
24	chr10:21982589-21982639	MCF-7	breast:	n/a
25	chr10:21958473-21958523	AG09309	skin:	n/a
26	chr10:21926911-21926961	SK-N-MC	brain:	n/a
27	chr10:21958473-21958523	PANC-1	pancreas:	n/a
28	chr10:21926911-21926961	HAEpiC	amniotic membrane:	n/a
29	chr10:21958473-21958523	T-47D	breast:	n/a
30	chr10:21926911-21926961	CMK	blood:	n/a
31	chr10:21982589-21982639	MCF10A-Er-Src	breast:	n/a
32	chr10:21926911-21926961	HEK293	kidney:	embryo
33	chr10:21926911-21926961	HCT-116	colon:	n/a
34	chr10:21926911-21926961	MCF-7	breast:	n/a
35	chr10:21982589-21982639	IMR90	lung:	fetal
36	chr10:21926911-21926961	ECC-1	luminal epithelium:	n/a
37	chr10:21982589-21982639	PrEC	prostate:	n/a
38	chr10:21982589-21982639	Jurkat	blood:	n/a
39	chr10:21982589-21982639	Hepatocyte	liver:	n/a
40	chr10:21958473-21958523	Jurkat	blood:	n/a
41	chr10:21958473-21958523	HEK293	kidney:	embryo
42	chr10:21958473-21958523	GM12891	blood:	n/a
43	chr10:21958473-21958523	RPTEC	kidney:	n/a
44	chr10:21958473-21958523	HRPEpiC	eye:	n/a
45	chr10:21926911-21926961	AoSMC	blood vessel:	n/a
46	chr10:21958473-21958523	AG09319	gingival:	n/a
47	chr10:21958473-21958523	BE2_C	brain:	n/a
48	chr10:21958473-21958523	Hela-S3	cervix:	n/a
49	chr10:21958473-21958523	HepG2	liver:	n/a
50	chr10:21926911-21926961	HPAEpiC	pulmonary alveolar:	n/a

(count:109 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr10:22008975..22011385-chr10:22011817..22013721,2	K562	blood:
2	chr10:21964215..21964716-chr10:22020856..22021759,2	MCF-7	breast:
3	chr10:22008975..22011385-chr10:22011817..22013721,2	K562	blood:
4	chr10:21996482..21998429-chr10:22004832..22006508,2	K562	blood:
5	chr10:21896692..21901028-chr10:21902485..21907046,7	K562	blood:
6	chr10:21963187..21965362-chr10:21971451..21973770,2	K562	blood:
7	chr10:21893811..21896382-chr10:21900964..21903749,2	MCF-7	breast:
8	chr10:21954505..21956388-chr10:21958814..21960336,2	K562	blood:
9	chr10:21784668..21785216-chr10:21964281..21964790,2	K562	blood:
10	chr10:21815978..21818479-chr10:21973475..21976355,2	K562	blood:
11	chr10:21814835..21816924-chr10:22010662..22012545,2	K562	blood:
12	chr10:21784864..21786534-chr10:22012885..22015848,2	K562	blood:
13	chr10:21897571..21899639-chr10:21900694..21903456,3	K562	blood:
14	chr10:21813812..21816552-chr10:22000725..22002586,2	K562	blood:
15	chr10:21817690..21818555-chr10:21919238..21919922,2	MCF-7	breast:
16	chr10:21976494..21979598-chr10:21980267..21982775,3	K562	blood:
17	chr10:21935621..21937602-chr10:21954791..21956548,2	K562	blood:
18	chr10:21816369..21819253-chr10:22004806..22007546,2	MCF-7	breast:
19	chr10:21932966..21934847-chr10:21935882..21937587,2	K562	blood:
20	chr10:21893811..21896382-chr10:21900964..21903749,2	MCF-7	breast:
21	chr10:21892363..21894156-chr10:21920730..21923308,2	MCF-7	breast:
22	chr10:21897294..21899834-chr10:21908105..21909643,2	MCF-7	breast:
23	chr10:21956427..21959026-chr10:21960604..21963223,2	K562	blood:
24	chr10:21927290..21929661-chr10:21936208..21938819,2	K562	blood:
25	chr10:21814516..21816347-chr10:22008760..22011406,3	MCF-7	breast:
26	chr10:21815711..21818489-chr10:22009525..22012289,2	MCF-7	breast:
27	chr10:21918257..21921849-chr10:21923696..21927257,3	K562	blood:
28	chr10:21919335..21919967-chr10:21931821..21932370,2	MCF-7	breast:
29	chr10:21822599..21824168-chr10:21898203..21900268,2	K562	blood:
30	chr10:21963187..21965362-chr10:21971451..21973770,2	K562	blood:
31	chr10:21813084..21814597-chr10:21884150..21887122,2	K562	blood:
32	chr10:21883151..21884959-chr10:21942105..21944413,2	K562	blood:
33	chr10:21909889..21911580-chr10:21929468..21932103,2	K562	blood:
34	chr10:21784768..21786630-chr10:21978936..21981188,2	K562	blood:
35	chr10:21821287..21825270-chr10:21999299..22001760,3	MCF-7	breast:
36	chr10:21909487..21912918-chr10:21916062..21919904,3	K562	blood:
37	chr10:21967381..21969902-chr10:21970354..21972033,2	K562	blood:
38	chr10:21912943..21915292-chr10:21917187..21920065,2	K562	blood:
39	chr10:21784221..21786507-chr10:22002819..22005576,2	MCF-7	breast:
40	chr10:21977667..21979449-chr10:21980673..21982775,2	K562	blood:
41	chr10:21601939..21603985-chr10:22012323..22013912,2	MCF-7	breast:
42	chr10:22007575..22010165-chr10:22014123..22016701,2	K562	blood:
43	chr10:21847924..21850525-chr10:22012351..22015305,2	MCF-7	breast:
44	chr10:21905679..21908459-chr10:21909977..21914285,3	K562	blood:
45	chr10:21927550..21928181-chr7:116231910..116232467,2	MCF-7	breast:
46	chr10:21970179..21972315-chr10:21973680..21976595,2	K562	blood:
47	chr10:21822599..21824193-chr10:21898159..21900268,3	K562	blood:
48	chr10:21998093..21999865-chr10:22003960..22005840,2	K562	blood:
49	chr10:21822403..21823988-chr10:21916839..21919635,2	MCF-7	breast:
50	chr10:22008261..22010475-chr10:22011835..22013721,3	K562	blood:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C10orf140-1	chr10:21913521-21915215	NONHSAT011721

No data

(count:1 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	MLLT10	hsa-miR-132-3p	chr10:21940668-21940686

Variant related genes	Relation type
MLLT10	TF binding region
RNU6-1141P	TF binding region
HNRNPRP1	TF binding region
MLLT10	CpG island
RNU6-1141P	CpG island
HNRNPRP1	CpG island
ENSG00000223984	chromatin interactions
ENSG00000242622	chromatin interactions
ENSG00000222071	chromatin interactions
ENSG00000078403	chromatin interactions
ENSG00000180592	chromatin interactions
ENSG00000204682	chromatin interactions

Extended variants
information (count: 4811 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:4811 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35587371	chr10:21878144-21878145	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs555841170	chr10:21878155-21878156	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs576096839	chr10:21878159-21878160	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs116199659	chr10:21878206-21878207	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs561940923	chr10:21878211-21878212	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs527510957	chr10:21878228-21878229	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs540809896	chr10:21878245-21878246	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs201960289	chr10:21878254-21878255	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs564079913	chr10:21878256-21878257	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs533053451	chr10:21878257-21878258	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs186200096	chr10:21878260-21878261	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs569908316	chr10:21878264-21878265	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs189508838	chr10:21878276-21878277	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs549241182	chr10:21878394-21878395	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs12783517	chr10:21878407-21878408	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs535276612	chr10:21878425-21878426	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs544253344	chr10:21878522-21878523	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs533364997	chr10:21878523-21878524	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs558382598	chr10:21878525-21878526	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs571973661	chr10:21878534-21878535	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs551759313	chr10:21878610-21878611	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs537701164	chr10:21878618-21878619	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs556140488	chr10:21878634-21878635	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs560431075	chr10:21878644-21878645	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs531206918	chr10:21878670-21878671	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs575919660	chr10:21878717-21878718	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs181342327	chr10:21878726-21878727	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs555205086	chr10:21878761-21878762	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs571796868	chr10:21878780-21878781	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs144962376	chr10:21878832-21878833	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs529529040	chr10:21878838-21878839	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs71393911	chr10:21878849-21878850	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs555988158	chr10:21878860-21878861	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs370679275	chr10:21878861-21878862	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs113813236	chr10:21878864-21878865	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs148487674	chr10:21878893-21878894	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs577523534	chr10:21878954-21878955	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs78381321	chr10:21878984-21878985	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs543315062	chr10:21878988-21878989	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs75630325	chr10:21878993-21878994	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs77318326	chr10:21879005-21879006	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs78138602	chr10:21879008-21879009	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs75407244	chr10:21879010-21879011	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs76488933	chr10:21879023-21879024	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs79641370	chr10:21879027-21879028	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs74835460	chr10:21879035-21879036	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs79549113	chr10:21879048-21879049	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs79910505	chr10:21879052-21879053	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs79397248	chr10:21879058-21879059	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs563720484	chr10:21879078-21879079	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:51)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Intracranial aneurysm	16715129	CNVD
Multiple myeloma	16616336	CNVD
T-cell lymphomas	19863542	CNVD
Esophageal cancer	21851588	CNVD
small cell lung cancer	20016488	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	21525872	CNVD
Intracranial arachnoid cysts	20187927	CNVD
Cancer	17440070	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Acute myeloid leukemia	19651600	CNVD
Prostate cancer	18632612	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	17699850	CNVD
Ovarian cancer	17699850	CNVD
Acute lymphoblastic leukemia	18458336	CNVD

Chromatin state (count:3524 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:21824600-21930400	Weak transcription	Gastric	stomach
2	chr10:21839400-21878200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr10:21839800-21880200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr10:21841200-21897200	Weak transcription	Fetal Kidney	kidney
5	chr10:21842200-21897200	Weak transcription	Fetal Brain Male	brain
6	chr10:21844600-21896600	Weak transcription	Hela-S3	cervix
7	chr10:21846800-21882200	Weak transcription	Brain Germinal Matrix	brain
8	chr10:21846800-21889600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr10:21846800-21892800	Weak transcription	HSMMtube	muscle
10	chr10:21846800-21913600	Weak transcription	Rectal Smooth Muscle	rectum
11	chr10:21847000-21901200	Weak transcription	HUVEC	blood vessel
12	chr10:21848800-21914200	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr10:21849400-21889600	Weak transcription	NHEK	skin
14	chr10:21849400-21913600	Weak transcription	Esophagus	oesophagus
15	chr10:21849800-21889400	Weak transcription	Brain Hippocampus Middle	brain
16	chr10:21849800-21894600	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr10:21849800-21897000	Weak transcription	Fetal Brain Female	brain
18	chr10:21850800-21889600	Weak transcription	HMEC	breast
19	chr10:21856800-21913400	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr10:21859400-21889800	Weak transcription	Pancreas	Pancrea
21	chr10:21860400-21886600	Weak transcription	Small Intestine	intestine
22	chr10:21860600-21879000	Weak transcription	Lung	lung
23	chr10:21860600-21895400	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr10:21860800-21878200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
25	chr10:21861200-21883000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr10:21861200-21890000	Weak transcription	Colon Smooth Muscle	Colon
27	chr10:21861400-21898400	Weak transcription	Brain Angular Gyrus	brain
28	chr10:21861400-21902800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
29	chr10:21861800-21878800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr10:21861800-21889600	Weak transcription	Brain Cingulate Gyrus	brain
31	chr10:21861800-21895400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr10:21861800-21898400	Weak transcription	Brain Anterior Caudate	brain
33	chr10:21861800-21913800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr10:21862200-21894200	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr10:21862400-21881600	Weak transcription	Stomach Smooth Muscle	stomach
36	chr10:21862400-21913600	Weak transcription	Adipose Nuclei	Adipose
37	chr10:21862400-21916400	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr10:21862800-21882000	Weak transcription	Ovary	ovary
39	chr10:21862800-21882200	Weak transcription	Primary T cells from cord blood	blood
40	chr10:21863800-21889000	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr10:21866000-21913600	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr10:21870200-21882600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr10:21870600-21889800	Weak transcription	NHLF	lung
44	chr10:21870600-21900600	Weak transcription	Right Ventricle	heart
45	chr10:21870800-21879800	Weak transcription	Primary B cells from peripheral blood	blood
46	chr10:21870800-21895000	Weak transcription	Osteobl	bone
47	chr10:21871000-21895000	Weak transcription	NH-A	brain
48	chr10:21871600-21880200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
49	chr10:21872200-21882200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr10:21872200-21897800	Weak transcription	Primary neutrophils fromperipheralblood	blood

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